Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_assertion evidence source_evidence_literature NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_assertion SIO_000772 22166941 NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_assertion wasDerivedFrom befree-20140225 NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_assertion wasGeneratedBy ECO_0000203 NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP267308.RAWfGyNjSbt5CCtlXWQ7js-s8anptDokNKLYqB6GesfIc130_provenance.